Department of Rheumatology and Immunology, National Clinical Research Center for Geriatrics, and State Key Laboratory of Biotherapy, West China Hospital, and West China School of Basic Medical Sciences & Forensic Medicine, Sichuan University, and Collaborative Innovation Center for Biotherapy, Chengdu, China.
Front Immunol. 2020 Oct 8;11:02157. doi: 10.3389/fimmu.2020.02157. eCollection 2020.
The tripartite motif (TRIM) proteins have been intensively studied as essential modulators in various biological processes, especially in regulating a wide range of signaling pathways involved in immune responses. Most TRIM proteins have E3 ubiquitin ligase activity, mediating polyubiquitination of target proteins. Emerging evidence demonstrates that TRIM proteins play important roles in innate immunity by regulating pattern recognition receptors, vital adaptor proteins, kinases, and transcription factors in innate immune signaling pathways. Additionally, the critical roles of TRIM proteins in adaptive immunity, especially in T cell development and activation, are increasingly appreciated. In this review, we aim to summarize the studies on TRIMs in both innate and adaptive immunity, focusing on their E3 ubiquitin ligase functions in pattern recognition receptor signaling pathways and T cell functions, shedding light on the developing new strategies for modulating innate and adaptive immune responses against invading pathogens and avoiding autoimmunity.
三基序蛋白(TRIM)作为各种生物学过程中的重要调节剂,受到了广泛的研究,尤其是在调节涉及免疫反应的广泛信号通路方面。大多数 TRIM 蛋白具有 E3 泛素连接酶活性,介导靶蛋白的多泛素化。新出现的证据表明,TRIM 蛋白通过调节先天免疫信号通路中的模式识别受体、重要衔接蛋白、激酶和转录因子,在先天免疫中发挥重要作用。此外,TRIM 蛋白在适应性免疫中的关键作用,特别是在 T 细胞发育和激活方面,越来越受到重视。在这篇综述中,我们旨在总结先天免疫和适应性免疫中 TRIM 的研究,重点关注它们在模式识别受体信号通路和 T 细胞功能中的 E3 泛素连接酶功能,为调节针对入侵病原体的先天和适应性免疫反应并避免自身免疫提供新的策略。